BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    DEFLECTING GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KNEE INTERPOSITIONAL MINI-REPAIR SYSTEM (KIMRS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STELLARIS VISION ENHANCEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OPTIBOND XTR

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code KLE·May 27, 2014

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXX·November 15, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·September 5, 2010